International safety notice

fabian™ HFOi. N.° REF: 113001

Spain / AEMPS · ESP · Apr 28, 2022

Key facts

Title fabian™ HFOi. N.° REF: 113001
Regulator Spain / AEMPS
Country ESP
Brand fabian™ HFOi. N.° REF: 113001
Manufacturer Acutronic Medical Systems AG. Suiza.
Models 5.2.1, 113001, 08174, FSCA21-004, FSCA-21-004-FSN, FSCA-21-004, 28022, FSCA-21002, FSCA-21-002, 91.822.52.89, 2022-203, 21-002 and 3 more
Event type Safety Notice
Date Apr 28, 2022

At a glance

  • No Recall
  • Yes Field safety notice
  • 1–9 Matching device models in FDA data
  • 1–9 Matching catalog numbers in FDA data

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About International device safety notices

Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.

Source: National medical device regulators (as listed), compiled by Orca1

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